Radical-mediated nitrile translocation as the key step in the stereoselective transformation of 2-(4-chloro-2-cyanobutyl)aziridines to methyl cis-(1-arylmethyl-4-phenylpiperidin-2-yl)acetates.
about
LiAlH4 -Induced Selective Ring Rearrangement of 2-(2-Cyanoethyl)aziridines toward 2-(Aminomethyl)pyrrolidines and 3-Aminopiperidines as Eligible Heterocyclic Building Blocks.Syntheses of Tetrahydrobenzodiazepines via SN2-Type Ring-Opening of Activated Aziridines with 2-Bromobenzylamine Followed by Copper-Powder-Mediated C−N Bond Formation
P2860
Radical-mediated nitrile translocation as the key step in the stereoselective transformation of 2-(4-chloro-2-cyanobutyl)aziridines to methyl cis-(1-arylmethyl-4-phenylpiperidin-2-yl)acetates.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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name
Radical-mediated nitrile trans ...... selective transformation of 2-
@nl
Radical-mediated nitrile trans ...... phenylpiperidin-2-yl)acetates.
@en
type
label
Radical-mediated nitrile trans ...... selective transformation of 2-
@nl
Radical-mediated nitrile trans ...... phenylpiperidin-2-yl)acetates.
@en
prefLabel
Radical-mediated nitrile trans ...... selective transformation of 2-
@nl
Radical-mediated nitrile trans ...... phenylpiperidin-2-yl)acetates.
@en
P2093
P2860
P356
P1476
Radical-mediated nitrile trans ...... phenylpiperidin-2-yl)acetates.
@en
P2093
Karel Vervisch
Karl W Törnroos
Matthias D'hooghe
P2860
P304
P356
10.1039/C2OB07062F
P577
2012-03-13T00:00:00Z